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the alveolar wall fenestrations to reach the medullary
cavities of the alveolar bone (Garfunkel etal.1983).
2) Along the outer surface of the alveolar bone, below the
periosteum and crossing through the cortical cavities to
the medullary cavities of the alveolar cancellous bone
(Tagger etal.1994a; Tagger etal.1994b).
In both cases, the anesthetic penetrates the medullary
cavities of the alveolar cancellous bone (Fuhs etal. 1983;
Dreyer et al. 1983; Garfunkel et al. 1983; Smith and
Walton1983b; Tagger etal.1994a,1994b), thus infiltrating
wide areas of the bone under pressure and moving toward
the apex at some distance from the injection site (Garfunkel
etal.1983; Smith and Walton1983b). Furthermore, as it
reaches the vessels and capillaries of the medullary cavities, it is considered to be equivalent with an intravascular
injection (Smith et al. 1983c; Rawson and Orr II 1985;
Pashley 1986), although experiments in humans have
found that, compared with intravascular injection, blood
levels are 25–40% without a vasoconstrictor, 10–15% with
epinephrine, and 10–50% with felypressin (Cannell
etal.1993). In summary, the PDL technique functions in
much the same way as the intraosseous technique
(Garfunkel etal. 1983; Smith and Walton 1983b; Smith
et al. 1983c; Pashley 1986), but with lower levels of
anesthetic.
Factors that Determine Efficacy
Major Factors
1) The pressure exerted is essential for successful anesthesia.
Resistance during injection is highly indicative of successful anesthesia (Walton and Abbott1981; Smith and
Smith1983a) because the pressure is necessary for the
anesthetic solution to be distributed along the periodontal ligament and bone marrow to reach the apex
(Edwards and Head1989).
2) Use of pressure syringes (pistol- type). This type of syringe
is more successful than traditional cartridge-
type syringes
(Table18.1), thus reinforcing point 1 above. This point
reinforces the first point, since pressure syringes are
designed to exert more pressure during the injection
(Pashley1986; D’Souza etal.1987; Walmsley etal.1989),
to the extent that it is almost double (Table18.2).
3) Use of local anesthetic solutions with epinephrine. The
best results are observed with standard solutions of
lidocaine 2% with epinephrine 1:100
000 (Malamed1982;
Johnson etal.1985; Kim1986; Schleder etal.1988) and
1:80
000 (Gray and Rood 1987; Meechan 2002), and
articaine 4% with epinephrine 1:100
000 (Berlin
etal.2005).
Lidocaine 2% with epinephrine 1:50 000 (high concentration of epinephrine) also yields favorable results, which
are even better and last longer than pulpal anesthesia,
although they also increase the risk of adverse effects
(such as tachycardi, palpitations, or tremors) (Kaufman
etal.1984). This better result is due not only to the fact
that the vasoconstrictor retains the anesthetic by preventing its absorption, but also to the fact that epinephrine
partially reduces blood flow in the dental pulp, thus leading to a partial reduction in A delta nerve fiber impulses
(Edwards and Head1989).
Poorer results are observed with anesthetic solutions that
do not contain epinephrine (Malamed 1982; Kaufman
etal.1984; Kim1986; Gray and Rood1987; Meechan2002),
have low doses of epinephrine (1:200
000), or contain
weaker vasoconstrictors (norepinephrine, levonordefrin,
felypressin) (Malamed 1982; Kaufman etal. 1984,1994;
Johnson etal.1985).
Minor Factors
1) Treatments where efficacy is evaluated.
● The best results are observed with extractions, obtu-
rations, and periodontal procedures (Malamed1982;
Table18.1 Percentage ofsuccess withintraligamentary (periodontal ligament technique) anesthesia achieved withhigh- pressure
syringes (pistol- grip) or traditional cartridge syringes.
Reference High- pressure syringe Standard syringe Treatment
Malamed (1982) 89% (54/61) 82% (32/39) Ob, En, Ex, C
Smith and Walton (1983b) 65% (39/60) 62% (55/88) En
D’Souza etal. (1987) 72% (13/18) 50% (12/24) Cold
Proportion 75% 65%
Ob, obturation; En, endodontics; Ex, extraction; C, cutting.
Cold, dry ice stimulation.
2
χ
=3.9537(P < 0.05).
Success (proportion)
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Table18.2 Maximum pressures achieved withstandard high- pressure syringes (pistol- type) inthe PDL andinfiltrative techniques.
Pressure
Factors evaluated PSI kg/cm
Maximum pressure achieved
Anesthetic technique Type of syringe
PDL Traditional 340 23.9 Pashley etal. (1981)
Traditional 325 22.8 Walmsley etal. (1989)
The Wand 232 16.0 Nusstein etal. (2005a)
The Wand STA
High-
pressure 616 43.3 Walmsley etal. (1989)
Infiltrative Traditional 153 10.8 Maita and Horiuchi (1984)
The Wand STA
Palatal injection The Wand STA
Mandibular block The Wand STA
Cartridges: resistance to breakage
Glass 1474 101.2 Meechan etal. (1990)
Plastic 655 45.2 “
kg/cm2, kilograms per square centimeter; PDL, periodontal ligament; PSI, pounds per square inch.
1 kg/cm2=14.5PSI; 1PSI=0.069kg/cm2.
a
The Wand STA injection 0.005 ml/second, mean pressure values.
a
a
a
a
294 20.3 Hochman etal. (2006)
11.5 0.8 Hochman etal. (2006)
68 4.7 Hochman etal. (2006)
5 0.35 Hochman etal. (2006)
2
Reference
Faulkner 1983; Kaufman et al. 1983; Miller 1983;
Grundy 1984; Gray and Rood 1987), undoubtedly
because these procedures require less deep pulpal
anesthesia (Handler and Albers1987; Walton1990).
● The poorest results are observed with endodontic proce-
dures (Malamed 1982; Faulkner 1983; Kaufman
etal.1983; Miller1983; Grundy1984) and tooth cutting
(Malamed 1982; Kaufman et al. 1983; Miller 1983)
because these approaches require deep pulpal anesthesia.
2) Teeth in which a PDL injection is made. Thus, the worst
results are noted for the anterior teeth (incisors and
canines) and the best results in the posterior teeth (molars
and premolars) (Kaufman etal.1983; White et al. 1988;
Meechan2002). These data are also shown in Table18.3.
3) The clinician’s experience with this technique also
improves on the results of clinical trials (Grundy1984).
Instrument Set
The PDL technique can be performed with the traditional
instrument set or with a more specific set, which is worthy
of analysis in terms of both syringes and needles.
Syringes
1) Traditional syringe. This is the classic cartridge- type
metal syringe, although it has certain disadvantages
with respect to the PDL technique: (i) it exerts half the
pressure of a high-
pressure syringe (pistol- type)
(Table18.2), therefore its anesthetic effect is reduced
(Table18.1) given that pressure is a key factor for the
success of this technique; (ii) women tend to exert 30%
less pressure than men with the traditional syringe
(Walmsley etal.1989); and (iii) if the cartridge breaks
because of excess pressure, the syringe does not have
the security foil that high- pressure syringes have to prevent glass fragments from falling into the patient’s
mouth (Malamed1982; Miller1983).
2) Pen- type high- pressure syringe (Citoject®) (Figure18.3).
This type of high- pressure syringe is easier to hide in
the hand, with the result that it is less “threatening” for
the patient (Primosch1986), although it is less stable
and requires considerable pressure with the fingers
(Cowan1986). Each trigger pull injects 0.06 ml. In terms
of clinical efficacy, this syringe is 65% successful as a
primary technique (Cowan1986).
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Table18.3 Percentage ofpulpal anesthesia, evaluated using anelectrical pulp tester, after administration ofthe standard solution
(L-
100) withthe PDL technique anda high- pressure pistol- type syringe inthe maxillary teeth (max) andmandibular teeth (mand).
Adjacent teeth
Tooth Reference Sample size Pulpal anesthesia Duration (min) Mesial Distal
Molars and premolars (M and PM)
First M max White etal. (1988) 20 75% 7 45% 60%
First M mand White etal. (1988) 38 79% 6 33% 62%
Cohen etal. (1993)
First PM max White etal. (1988) 24 58% 4 17% 42%
First PM mand Handler and Albers (1987) 7 57% 22 —
Moore etal. (1987) 19 79% 10 16% 63%
Schleder etal. (1988) 75 87% 20 45% 78%
White etal. (1988) 39 63% 8 21% 45%
McLean etal. (1992) 24 38% 12 —
Meechan (2002) 16 79% 16 — —
Second PM D’Souza etal. (1987)
Incisors and canines (LI, C)
C max Johnson etal. (1985) 20 35% 10 — —
LI max White etal. (1988) 23 39% 16 30% 26%
Kaufman etal. (1994) 40 50% 5 —
Meechan (2002) 16 75% 16 — —
LI mand White etal. (1988) 22 18% 7 9% 9%
C max Johnson etal. (1985) 20 55% 17 —
a
10 80% — — —
—
—
b
42 60% — — —
Average 68.6% 11.7 30% 58%
Rounded average 70% 10
—
—
Average 45.3% 11.8 20% 18%
Rounded average 45% 10
The table also shows the extension to adjacent teeth both mesially and distally.
L- 100 is the standard solution of lidocaine 2% with epinephrine 1:100 000 (10 μg/ml).
a
Cold stimulus with dichlorodifluoromethane in irreversible pulpitis, instead of an electric pulp tester.
b
Cold stimulus with carbon dioxide, instead of an electric pulp tester.
Figure18.3 High- pressure pen- type syringe (Citojet®).
3) Pistol- type high- pressure syringe (Ligmaject® and
Peripress® or similar syringes) (Figure18.4).
This type of syringe first appeared in the 1970s. It has a
pistol grip and a barrel with a lateral window that enables
the clinician to see how much solution remains in the cartridge and any possible breakage in the cartridge
(Primosch 1986). The syringe has a Mylar sheath that
encases the cartridge in the barrel to prevent pieces of glass
from entering the patient’s mouth in the case of breakage
(Khedari1982; Malamed1982; Miller1983; Saadoun and
Malamed1985; Primosch1986). It is important to remember that with this technique the cartridge can break in 1.5%
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● Tooth (pulp and periodontal ligament) on which the
technique is performed, extending mesially– and more
often distally– to the adjacent teeth.
● Vestibule and tongue area, both the fibromucosa (alveo-
lar mucosa, gum, and interdental papillae) and the bone
and periosteum of the anesthetized tooth. It is important
to remember that this technique is applied in a very welldefined area.
Figure18.4 High- pressure pistol- type syringe (Ligmaject® or
Peripress®).
of cases (Primosch1986). Each trigger pull injects 0.2 ml of
the anesthetic solution (Council on Dental Materials,
Instruments, and Equipment1983).
The pistol grip provides better control and stability, thus
enabling the following: (i) application of considerable pressure (Chenaux et al. 1976; Khedari1982; Pashley 1986;
D’Souza et al. 1987), almost twice that of a traditional
syringe (Table 18.2), and (ii) a measurable difference in
applied pressures between male and female providers has
not been detected (Walmsley etal. 1989). Therefore, as a
primary technique, this type of syringe has a success rate of
75% (Table18.1).
Needles
Traditional cartridge- type syringes require 27G or 25G
short needles (20–25
mm). Since 25G needles are more
rigid, they are easier to manage (Walton and Abbott1981;
Malamed1982; Walton1990).
High-
pressure syringes require 30G or 27G extrashort
needles (8–12
mm), and although the 30G needle is the
most widely used, it is also the caliber that most frequently
bends under the pressure applied during injection
(Malamed 1982; Smith and Smith 1983a). Therefore, the
extrashort 27G needle (8 mm) is preferable, since it bends
less and is sufficiently fine to fit between the tooth and the
alveolar crest.
Cartridges
Glass cartridges are preferred because they can bear twice
as much pressure as plastic cartridges before breaking
(Table18.2). Plastic cartridges do not break, although they
deform at half the pressure of a glass cartridge, thus enabling the anesthetic solution to leak out (Meechan
etal.1990).
Anesthetized Area
The area anesthetized with the PDL technique is welldefined, as in all supplementary techniques.
Technique
● If a dental dam is in place, then it must not be removed
(Nusstein etal.2003). This is an advantage.
● As a primary technique, this approach is considered
painful (Annex 23), but it is not painful in practice
because it is used as a supplementary technique when all
other approaches have failed and therefore all the adjacent
tissues, but not the dental pulp, are anesthetized.
● Given our previous comments, the most advisable
approach would be to use a pistolsyringe with an extrashort 27G needle (8
type high- pressure
mm) and a local
anesthetic solution with epinephrine (if there are no
contraindications), similar to the one being used in the
area (remember not to mix two different anesthetic solutions at the same site). For example, if articaine 4% with
epinephrine 1:100
000 (A- 100) is used in a buccal maxillary infiltration, then the same solution should be
injected; if a mandibular block is performed with standard lidocaine 2% with epinephrine 1:100
then reinforced with a buccal infiltration a of Athen the procedure should be continued with A-
000 (L- 100) and
100,
100 in
the intraligamentary technique.
● Clean the gingival area of food particles, debris, plaque,
or tartar beforehand (Chenaux et al.1976; Brännström
et al. 1982; Kaufman et al. 1983; Council on Dental
Materials, Instruments, and Equipment1983; Faulkner
1983) to prevent them from entering the tissues.
● Insert the needle into the gingival sulcus. This is the
most important step, and often the most difficult (Council
on Dental Materials, Instruments, and Equipment1983).
○ Insert the needle mesially into the mesial- buccal and
mesial- lingual angles, distally into the distal- vestibular
and distal- lingual angles (Figure18.5).
○ With an angle of approximately 30° with respect to the
axis of the tooth to respect the convexity of the enamel
of the neck of the tooth (Figure18.6).
○ The bevel should be facing outwards.
○ The needle should be forced firmly between the alveolar
crest and the cervical surface of the root of the tooth,
pressing toward the apex.
○ It is occasionally necessary to bend the stem of the
needle to reach the most posterior teeth (Chenaux
etal.1976; Khedari1982; Primosch1986).
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Figure18.5 Mesio- vestibular, mesio- lingual, disto- vestibular,
https://t.me/med1917
and disto- lingual angles where the needle is inserted.
30°
Figure18.6 30° angle with respect to the axis of the tooth for
insertion of the needle. Note that the bevel is turned outwards.
● Aspiration is not necessary since the anesthetic solution,
once injected, is thought to reach the systemic bloodstream quickly (Smith and Walton1983b; Rawson and
325
Orr II1985). Some clinical trials report positive aspirations in 94% of cases (Medvedev etal.2012).
● Inject under pressure.
○ Pressure is very important for the success of the tech-
nique and is a sign that the needle has been inserted
correctly (Walton and Abbott 1981; Smith and
Smith1983a). If the injection is made at several points
in a tooth, then there should be resistance to the injection in at least one point. If there is no resistance, then
the anesthetic solution has been distributed through
the soft tissue but has not reached the apex.
○ If there is no resistance, remove the needle and reposi-
tion it by reinserting it and forcing it toward the apex
(Khedari1982).
○ Pressure should be maintained at each point for
10–20
seconds while injecting slowly (Meechan1992) in
order to:
◼ Prevent excess pressure from breaking the cartridge.
◼ Ensure that the anesthesia penetrates the tissue,
preventing reflux of the anesthetic into the mouth.
Despite these measures, some of the anesthetic
often flows back into the patient’s mouth, and in
70% of cases he/she notices the bitter taste of the
solution (Grundy1984).
○ The gum adjacent to the injection point turns white
and pale owing to the ischemic effect of the pressure
and the vasoconstrictor.
● Amount to be injected.
○ Each trigger pull injects 0.2 ml (Chenaux etal.1976;
Council on Dental Materials, Instruments, and
Equipment1983). Thus:
◼ In monoradicular teeth, the solution is injected into
one or two of the abovementioned sites mesially
and/or distally (total 0.2–0.4 ml).
◼ In the case of multirooted teeth, the solution is
injected at two or four sites mesially and distally
(total 0.4–0.8 ml).
○ These amounts are indeterminate since an unknown
quantity of solution flows back into the patient’s mouth.
● Onset of pulpal anesthesia is very fast (10–30 seconds)
(Walton and Abbott1981; Kaufman etal.1983; Gray and
Rood1987; White etal.1988; Childers etal.1996). In 93%
of cases where anesthesia is successful, the pulp is already
anesthetized at 15 seconds (Walton and Abbott1981). The
anesthetic effect has a short duration, on average 10 minutes
(Table18.3) and generally less than 20 minutes (Childers
etal.1996).
○ As the effect is very localized and there are scarcely
any subjective symptoms (soft tissue anesthesia), the
only guarantee of success is treatment. If the technique is used as a supplementary approach (the most
common situation), the soft tissue anesthesia is from
the techniques that have failed.
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○ As primary anesthesia (very uncommon), anesthesia of
the soft tissues lasts 25–40
● If the approach fails, a new attempt can be made after
30–60
seconds (Cohen etal.1993), thus improving the
minutes (Johnson etal.1985).
results (Table18.4). There is generally no risk of toxicity,
even though the technique is considered to inevitably
result in intravascular administration, since the dose
administered is small and the technique is only used in
specific teeth when standard techniques have failed.
Moreover, part of the injected solution flows back into
the mouth.
Efficacy ofThis Technique
The efficacy of the technique is evaluated using an electric
pulp tester, which tells us that the success rate is 70% in
posterior teeth and 45% in anterior teeth, with a duration of
around 10
minutes (Table18.3). These data are for pistoltype high- pressure syringes and a single injection of standard solution (L-
100). Furthermore, we can observe that the
neighboring teeth are also anesthetized, especially the distal teeth (Table18.3). Evaluation of clinical success (more
subjective and less rigorous method) reveals a success rate
of 90%, although this can be with one or two injections
(two if the first fails) (Tables18.4 and18.5).
Table18.5 Percentage ofclinical success withthe periodontal
ligament injection using apistolinjection solution (L-
Reference Sample size Treatment Success
Malamed (1982) 100 Ob, Ex, En, C 86%
Faulkner (1983)
Kaufman etal. (1983) 258 Ob, Ex, En 84%
Miller (1983) 361 Ob, Ex, En, C 96%
Smith and Smith
(1983a)
Matthews and
Stables(1985)
Rakusin etal. (1986) 30 Ob 97%
Gray and Rood (1987) 48 Ob, Ex, En 92%
Edwards and Head
(1989)
L- 100, lidocaine 2% with epinephrine 1 : 100 000; Ob, obturation; En,
endodontics; Ex, extraction; C, cutting.
Success after one or two injections.
a
Local anesthetic solution unknown.
100).
a
type syringe andthe standard
200 Ob, Ex, En 86%
60 En 85%
100 — 86%
14 Ex 80%
Average 88%
Rounded average 90%
Specific Complications ofthe Technique
Complications Dueto Performance ofthe Technique
1) 30G needles usually bend because they are not very
rigid and it is necessary to apply a certain degree of
pressure (Malamed 1982; Kaufman etal. 1983; Smith
and Smith 1983a), therefore it is more appropriate to
Table18.4 Percentage ofsuccessful clinical outcome after
thefirst injection andafter thefirst andsecond injections, both
withpistol-
Reference Treatment
Smith and Walton
(1983b)
Gray and Rood
(1987)
Cohen etal. (1993) En 80% 90%
Cohen etal. (1993) En 70% 100%
Ob, obturation; En, endodontics; Ex, extraction.
type syringes.
First
injection
En 65% 85%
Ob, Ex, En 71% 92%
Average 72% 92%
Rounded average 70% 90%
Success
First and second
injection
use extrashort 27G needles in high-
pressure syringes
because these are more rigid and resistant. If the needle
bends, it should be replaced.
2) Reflux of the anesthetic solution into the patient’s
mouth is common. The patient experiences the bitter
taste in the case of solutions that contain vasoconstrictor (Malamed1982; Kaufman etal.1983). This occurs in
70% of cases in some series (Primosch1986).
3) Breakage of a glass cartridge due to excess pressure
(Malamed1982; Kaufman etal. 1983). This has been
reported in 1.5% of cases (Primosch1986). Thus, with
traditional cartridge-
type syringes, pieces of glass may
fall into the patient’s mouth (especially if the cartridges
do not have a transparent adhesive plastic protective
sleeve [security foil] that limits splintering; Rawson and
Orr II1985). The problem of glass entering the patient’s
mouth does not affect the high- pressure syringes used
in the PDL technique because they have a transparent
plastic sleeve that encases the cartridge in the barrel of
the syringe (Khedari1982; Malamed 1982; Miller1983).
Periodontal Abnormalities
The periodontium can be damaged for three reasons
(Brännström etal.1982; Peterson etal.1983): (i) mechanical damage caused by the needle, (ii) pressure of the injected
solution, and (iii) toxic effect of the solution.
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Studies with animals (mainly dogs and monkeys) and
gum dissection have shown lesser damage, mainly in the
bony crest and cementum and in the more coronal areas,
with reabsorption of the root (Roahen and Marshal 1984,
1990; Nakane and Kamayama1987). This type of damage
reverses in a few weeks (Brännström et al.1982; Walton
and Garnick1982; Dreyer et al.1983; Fuhs et al.1983;
Peterson et al. 1983; Galili et al. 1984; Albers and
Ellinger1988).
Clinical studies in humans have shown that there are no
periodontal sequelae after a few weeks (Malamed 1982;
Moore etal.1987; Schleder etal.1988). However, complications and exceptional cases may arise, as follows:
1) Pain after a PDL injection is very common (Kaufman
etal.1984; D’Souza etal.1987) and occurs in around 80%
of cases (Schleder etal.1988; White etal.1988; Nusstein
etal.2004). It is very intense in 5% of cases (Table18.6),
although it usually resolves spontaneously in 2–3 days.
2) Twenty percent of patients report feeling that the tooth
is high during occlusion (Table 18.6), although this
resolves spontaneously in a few days. If the feeling does
not improve, occlusion can be adjusted (Malamed1982).
There have been reports of two extreme cases of teeth
that were ejected after the PDL injection: a first mandibular premolar (Nelson 1981) and a mandibular
molar (Council on Dental Materials, Instruments, and
Equipment1983), both of which were healthy.
3) A certain degree of gingival inflammation appears in 5%
of cases (Table18.6). This resolves spontaneously in a
few days, and, if it lasts longer, chlorhexidine mouth
rinses and antibiotics can be administered. Three
extreme cases have been reported: an upper molar with
recession of the root that required endodontic treatment (White etal.1988), a molar with marginal papillitis and necrosis (Kaufman et al.1983), and a molar
with inflammation of the gum, loss of 50% of bone, and
pockets measuring 6–8 mm treated with scaling and
root planning and antibiotics for 8 months (Childers
etal.1996).
Pulpal Abnormalities
Dissections of teeth in experimental animals revealed no
histological changes or damage in dental pulp (Roahen and
Marshall 1984, 1990; Peurach 1985; Albers and
Ellinger1988; Walton1990; Plamondon et al.1990). The
same observation was reported for humans (Torabinejad
etal. 1993). Some experimental studies revealed reduced
pulpal blood flow due to the action of epinephrine in the
injection (Kim1986).
Clinical studies in humans have not reported pulpal
abnormalities (Malamed1982; Moore etal.1987; Schleder
etal.1988), except for the case of pulpal abnormality in a
cut tooth (Kim1986). We do not know whether the PDL or
the cutting caused the problem.
Table18.6 Percentage ofperiodontal complications withthe periodontal ligament injection.
Reference Sample size Severe postinjection pain High tooth feeling Gum inflammation
Malamed (1982) 100 3% 2% —
Kaufman etal. (1983) 258 2% — 0.4%
Faulkner (1983) 200 —
Grundy (1984) 361 9% — —
Matthews and Stables(1985) 100 11% — —
Johnson etal. (1985) 20 — — 5%
Rakusin etal. (1986) 32 10% —
Davidson and Craig (1987) 100 8% — —
List (1988) 22 — 27% —
Schleder etal. (1988) 75 5% 49% 5%
Spuller (1988) 28 —
White etal. (1988) 147 2% — —
McLean etal. (1992) 48 2% 13% —
Nusstein etal. (2004) 51 3% 27% 8%
Average 5.5% 20.2% 4.2%
Rounded average 5% 20% 5%
— 2.5%
—
3.5% —
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Cardiovascular Abnormalities
The PDL technique is considered almost intravenous since
the anesthetic solution passes very quickly to the bloodstream. Experiments with dogs revealed a 20% fall in arterial pressure and a 20% increase in heart rate (Smith and
Pashley1983d; Pashley1986).
Clinical trials with anesthetic solutions containing epinephrine 1:100
Nusstein etal. 2004) and 1:80
000 (10 μg/ml) (Kaufman et al. 1994;
000 (12.5 μg/ml) (Gray and
Rood 1987) did not reveal appreciable modifications in
arterial pressure or heart rate. However, the use of higher
concentrations of epinephrine (1:50
000, 20 μg/ml) leads to
an increase in heart rate (tachycardia), which patients
describe as palpitations, in 20% of cases (Kaufman
etal.1984).
Intraseptal Technique
The intraseptal technique, also known as the crestal technique (Giffin1994) or papillary technique (Marthaler1970),
involves inserting the needle into the interdental papilla to
reach the septum (where the cortical plate is very narrow
or has disappeared [Marthaler1970] and which is the exit
for a large number of miniperforations that finish in the
medullary cavity [Saadoun and Malamed1985]) and penetrating a few millimeters with the tip of the needle to
inject the anesthetic solution under pressure into the cancellous bone so that it spreads quickly to the apex of the
tooth. In practical terms, this approach is a variant of the
PDL injection; in addition, during the PDL injection, the
needle very often becomes stuck in the alveolar crest
instead of in the gingival sulcus, and the solution is injected
into the interdental septum under pressure.
The intraseptal technique was already well known in the
1940s (Nevin and Puterbaugh1949). It was recovered by
Marthaler in the 1970s (Marthaler1970).
Factors Underlying aSuccessful Technique
1) The use of pistol- type high- pressure syringes, such as
those used in the PDL (Ligmaject® or Peripress®),
because they enable high- pressure continuous and uniform injection (Saadoun and Malamed1985).
2) 27G extrashort needles (8–12 mm), which are some-
what thicker than the 30G needles, since these are sufficiently rigid so as not to bend during injection under
pressure and sufficiently fine to penetrate the intraseptal bone (Saadoun and Malamed1985; Giffin1994).
3) The use of local anesthesia solutions with vasoconstric-
tor, such as lidocaine 2% with epinephrine 1:100 000
(Giffin1994) or 1:50 000 (Saadoun and Malamed1985).
Contraindications
The contraindications are the same as those of the PDL
technique, as follows:
1) In primary teeth, there is a risk of permanently damag-
ing the tooth (Alantar1993).
2) In the case of teeth with advanced periodontal disease,
the periodontal structures may be affected. This point is
under debate because some authors consider it a contraindication (Alantar 1993), whereas others do not
(Saadoun and Malamed1985). As is the case with the
PDL injection, teeth affected by periodontal disease that
are to be extracted constitute an exception.
3) Infection at the injection site.
Anesthetized Area
● Tooth (pulp and periodontal ligament) on which the
technique is applied, although the area anesthetized frequently extends to the adjacent teeth mesially and distally. The results are not known with any degree of
accuracy, although they are considered to be similar to
those of the PDL technique (Giffin 1994), with a lower
percentage of success in the anterior teeth (Giffin1994)
and a shorter duration of pulpal anesthesia.
● Vestibule and lingual area, both in the fibromucosa
(alveolar mucosa, gum, and interdental papillae) and in
the bone and periosteum along a limited band measuring approximately 20–25
mm in length (Saadoun and
Malamed1985). Anesthesia lasts less than an hour.
Technique
● Select the insertion site in the center of the interdental
papilla close to the tooth to be anesthetized. The inser-
tion site is at the midpoint of the papilla between the
teeth and exactly 2
● Place the needle vertically at an angle of approximately
mm under the cusp of the papilla.
45° with respect to the axis of the tooth and horizontally
perpendicular to the papilla (Figure18.7).
In posterior mandibular teeth, it may be necessary to
bend the needle some 45° along the stem to ensure correct
positioning.
● Insertion of the needle:
○ Inject a few drops into the fibromucosa of the papilla
after inserting the needle.
○ Advance the needle until it makes contact with the
alveolar bone crest and continue to apply pressure so
that the needle crosses the weak point of the cortical
plate at this level and reaches the cancellous bone. In
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45°
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Figure18.7 Insertion of the needle into the interdental
septum at an approximate angle of 45°, with penetration of the
cancellous bone.
329
● Aspiration is not performed, since this technique,
as with the PDL injection, is considered almost
intravascular.
● Anesthesia is almost immediate, less than 15 seconds
(Saadoun and Malamed1985). It is restricted to the tooth
and the surrounding area, and the patient has no subjective sensation of paresthesia in the soft tissues. If anesthesia has not been achieved after 30
seconds, then the
technique has failed and must be restarted (Saadoun and
Malamed1985).
Specific Complications ofthe Technique
1) Pain during the injection in more than 25% of cases,
when it is used as the primary technique (Saadoun and
Malamed 1985), although in practice it is used as a
supplementary technique in cases of failure, when the
tissues are already anesthetized.
2) Patients often complain of palpitations (tachycardia)
owing to the use of anesthetic solutions containing epinephrine (Saadoun and Malamed1985; Giffin1994).
3) Postinjection pain at the injection site in 20% of cases,
although this disappears spontaneously in 1 or 2 days
(Giffin1994).
total, the needle can penetrate 2–3 mm into the bone
tissue (Figure18.7).
○ Withdrawing the needle 1 mm and rotating the syringe
helps the needle to penetrate the bone (Saadoun and
Malamed1985).
● Inject 0.2–0.4 ml of anesthetic solution (Saadoun and
Malamed1985; Alantar1993; Giffin1994).
○ The solution is injected under pressure so that the anes-
thetic penetrates the medullary spaces. In addition, it
is injected slowly (0.2 ml in 20–30 seconds) to prevent
excess pressure from breaking the cartridge.
○ The ischemia caused by the pressure of the injection and
the vasoconstrictor in the solution leads to blanching.
○ If the injection is very fluid and there is no pressure,
then the needle is not penetrating the bone and the
distribution of the solution is limited to the soft tissue
or may even flow back into the mouth (in this case the
patient notices the bitter taste of the solution [Saadoun
and Malamed1985]). The needle should then be withdrawn and repositioned in the papilla before starting
the procedure again.
○ If the injection seems difficult and the needle does not
advance despite pressure, then it has reached an area
of thick cortex or is poorly angled, thus preventing it
from entering the cancellous bone. In this case, the
needle should be withdrawn and repositioned in the
papilla before starting the procedure again.
Intraosseous Technique
This technique is also known as the intradiploic or transcortical technique. It involves crossing the cortex with a
drill and using a needle to inject the anesthesia into the
cancellous bone close to the tooth to be anesthetized in
such a way that it spreads rapidly toward the apex.
The technique was first applied by Otte in 1896
(Smith 1920) or by R. Nogué in 1907 (Nogué 1907) (we
were unable to verify which of the two was first) and then
by Masselink in 1910 (Masselink1910). In these early techniques, the bone was perforated with round burrs (thus
making it difficult to maintain the perforation straight) and
the solution was injected with a thick cannula to prevent
reflux (Masselink 1910; Parrot1914). During the 1930s,
the method became popular and dentists started to drill at
the level of the attached gingiva with straight burrs
(Schmitt1936; Nevin and Puterbaugh1949). In the 1940s,
Beutelrock perforators became popular; however, as these
were relatively long, they broke easily, and it was difficult
to extract them (Nevin and Puterbaugh1949). Consequently,
the Van den Berg system was developed (Leonard 1995;
Dunbar etal.1996; Peñarrocha et al. 1997); this involved
5- mm perforators with a stop to prevent overpenetration
and extrashort needles of the same caliber. Unfortunately,
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330
the perforator was too short (5 mm) and, very often, it was
not possible to completely perforate the cortical plate
(Roberts and Sowray1987). During the 1960s and 1970s,
few studies based on this technique were published
(Magnes1968; Bourke1974; Lilienthal1976).
The modern era began in 1991, when Frank Dillon devel-
®
oped the Stabident
designs and disposable materials, with a 9-
system, which incorporated new
mm drill and a
needle of the same caliber and length (Leonard 1995;
Dunbar etal.1996; Peñarrocha etal.1997). Later, in 1999,
®
Arthur Weather developed the X-
system, with charac-
Tip
teristics that are very similar to those of Stabident® but
which incorporates a guide sleeve so as not to lose the perforation when inserting the needle (Hawkins and
Moore2002). Some time later, Stabident® also incorporated
an optional guide sleeve. Other less popular variants began
to appear, such as a hand-
held device designed for this
technique, IntraFlow® (Kleber2003; Remmers etal.2008)
or Anesto (Graetz et al. 2013), and the hybrid system
known as QuickSleeper (Villette2003) (see Chapter20).
In this section, we provide a careful analysis of the
Stabident® and X-
Tip® systems because these are the most
important and most widely used.
Indications, Contraindications,
andDisadvantages
We have already mentioned the indications. The intraosseous technique is a supplementary technique that is only
used when standard techniques fail. In addition, it has two
disadvantages: (i) it requires a perforator and an extrashort
needle, and (ii) rubber dams must be removed to apply the
technique (one advantage of the PDL injection is that this
is not necessary). The contraindications of the technique
are as follows:
Instrument Set
In this section, we analyze the instruments used in the two
main systems, Stabident® and X-
Stabident®
Tip®.
This system is based on two elements, as follows (Stabident
instruction manual2001) (Figure18.8):
1) The perforator, or drill, which comprises a plastic shank
and has the following parts:
○ Plastic shank that is inserted into the contra- angle
hand piece.
○ Plastic stop that marks the depth of perforation and
is, at the same time, an adapter for the plastic protective cap that covers the metal needle of the perforator.
○ Solid 27G metal needle (0.43 × 9 mm) that comes out
of the plastic stop and is the active part of the perforator used to penetrate the cortical layer.
○ Plastic protective cap that covers the solid metal nee-
dle (or active end) and adapts to the plastic stop.
2) Extrashort 27G needle (0.4 × 8 mm) with dimensions
that are identical to those of the perforator and covered
by its corresponding sleeve.
The instrument is sufficiently long to cross the gum and
cortical bone, and thus reach the cancellous bone in most
cases. Table18.7 shows the thicknesses to be crossed by the
perforator. Since the distance would be greater than 8
mm
in only 2.5% of cases, the system has a longer reach than
the 5
mm of the old Van den Berg system.
1
1) Primary teeth, since the permanent tooth buds may be
damaged, although some authors have used the
approach in children (Magnes1968; Bourke1974).
2) Teeth with advanced periodontal disease since the tooth
may fall out accidentally during the procedure (Parente
etal.1998). Teeth to be extracted are an exception.
3) Infection with cellulitis or an abscess in the area to be
perforated since this would be very painful and deep
anesthesia may not be achieved (Reader et al. 2011;
Council on Clinical Affairs2015).
4) Areas with little cancellous bone, such as those between
the upper and lower central incisors (Lilienthal1975a)
and areas with very crowded teeth. As it is difficult to
drill in these areas, it is recommended to use the nearest
distal space. An alternative is to use the PDL injection
and not the intraosseous technique.
2
Figure18.8 Stabident® system with the perforator (1) and
needle (2).
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